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目的研究60例伴其他自身免疫性疾病的重症肌无力患者的临床特点。方法共60例重症肌无力患者,分为ADMG组(30例)和不伴其他自身免疫性疾病重症肌无力组(30例),通过对两组患者的发病年龄、性别、症状、肌无力危象、胸腺的异常、治疗活动的开展以及肌无力的状态和术后的恢复等情况的分析来对检测结果进行明确:即,肌无力现象所带来的眼肌型重症肌无力是全身型的重症表现。其往往在一年内会因重症复发,而没有开展统计的价值。结果通过对整个因素的分析,两组患者的性别差异值得关注。结论 ADMG组患者多见于青年女性,表现为眼肌型重症肌无力,并伴发胸腺增生。
Objective To investigate the clinical features of 60 patients with myasthenia gravis with other autoimmune diseases. Methods A total of 60 cases of myasthenia gravis patients were divided into ADMG group (30 cases) and other autoimmune diseases without myasthenia gravis group (30 cases). According to the age, sex, symptom, myasthenia gravis Elephant thymus abnormalities, the development of treatment activities and the state of muscle weakness and postoperative recovery of the analysis to determine the test results: muscle weakness caused by ocular myasthenia gravis is a systemic type Severe manifestation. It is often within a year due to recidivism, but did not carry out statistical value. Results Through the analysis of the whole factor, the gender differences of the two groups deserve attention. Conclusions The ADMG group is more common in young women with oculomotor myasthenia gravis and thymus hyperplasia.